SIGMA-ALDRICH MANUFACTURING, LLC-H&H FDA Inspection Record

FEI 1937990 · Inspections, Form 483s, warning letters and import refusals

SIGMA-ALDRICH MANUFACTURING, LLC-H&H is an FDA-registered facility (FEI 1937990) located in Saint Louis, MO, US. RegDataLab tracks 7 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Apr 28, 2025: Voluntary Action Indicated (VAI)
Inspections on record
7 (7 VAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Apr 28, 2025Voluntary Action Indicated (VAI)No citations listed
Feb 6, 2019Voluntary Action Indicated (VAI)No citations listed
Mar 10, 2017Voluntary Action Indicated (VAI)No citations listed
Dec 9, 2013Voluntary Action Indicated (VAI)Change records, content (21 CFR 820.40(b))
Jun 18, 2012Voluntary Action Indicated (VAI)No citations listed
Apr 19, 2011Voluntary Action Indicated (VAI)No citations listed
Sep 2, 2009Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
Sigma-Aldrich Manufacturing LLC
Location
Saint Louis, MO (US)
Source
device

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.